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Direct G protein modulation of Cav2 calcium channels.

机译:Cav2钙通道的直接G蛋白调节。

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摘要

The regulation of presynaptic, voltage-gated calcium channels by activation of heptahelical G protein-coupled receptors exerts a crucial influence on presynaptic calcium entry and hence on neurotransmitter release. Receptor activation subjects presynaptic N- and P/Q-type calcium channels to a rapid, membrane-delimited inhibition-mediated by direct, voltage-dependent interactions between G protein betagamma subunits and the channels-and to a slower, voltage-independent modulation involving soluble second messenger molecules. In turn, the direct inhibition of the channels is regulated as a function of many factors, including channel subtype, ancillary calcium channel subunits, and the types of G proteins and G protein regulatory factors involved. Twenty-five years after this mode of physiological regulation was first described, we review the investigations that have led to our current understanding of its molecular mechanisms.
机译:通过激活七螺旋G蛋白偶联受体来调节突触前电压门控的钙通道,对突触前钙的进入并因此对神经递质的释放具有至关重要的影响。受体激活使突触前的N和P / Q型钙通道受到快速的,膜界定的抑制作用,这种抑制作用是由G蛋白betagamma亚基和这些通道之间直接的,电压依赖性的相互作用介导的,以及一种较慢的,电压依赖性的调节,包括可溶的第二信使分子。反过来,对通道的直接抑制也受许多因素的调节,包括通道亚型,辅助钙通道亚基,以及涉及的G蛋白和G蛋白调节因子的类型。在首次描述这种生理调节模式后的二十五年,我们回顾了导致我们对它的分子机制的当前理解的研究。

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